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A Comparative Study of the Performance of a New Type Non-contact Patient Monitor

H

Holux Technology

Status

Unknown

Conditions

Indication for Modification of Patient's Cardiopulmonary Status

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01592877
Holux_SKH01

Details and patient eligibility

About

To verify the accuracy and reliability of the ultra wideband (UWB) non-contact breath rate and heart rate monitor, ICU bedside monitor is used as the gold standard.

Full description

In this study, 50 volunteer patients are tested on the UWB non-contact breath rate and heart rate monitor. The testing time length for each patient is set to two hours. Subject is not to be restrained and nurse is allowed to take care the subject while testing. The breath rate and heart rate data will be analyzed for their accuracy against the MP60 (Philips) bedside monitor.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • conscious adult,
  • > 18 years old

Exclusion criteria

  • non-conscious,
  • pregnant women,
  • epilepsy patients,
  • patients with heart pacemaker or ACIDS,
  • patients on respirator

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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